ZMP
hbegfb
Ensembl ID:
ZFIN ID:
Description:
heparin-binding EGF-like growth factor b [Source:RefSeq peptide;Acc:NP_001093871]
Human Orthologue:
HBEGF
Human Description:
heparin-binding EGF-like growth factor [Source:HGNC Symbol;Acc:3059]
Mouse Orthologue:
Hbegf
Mouse Description:
heparin-binding EGF-like growth factor Gene [Source:MGI Symbol;Acc:MGI:96070]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37340 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11891 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37340
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010193 | Nonsense | 108 | 239 | 3 | 6 |
ENSDART00000130676 | None | None | 113 | None | 4 |
ENSDART00000130820 | Nonsense | 132 | 263 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 21 (position 28910241)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 30129485 |
GRCz11 | 21 | 30166180 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATGCACTGACATCACTCTTGCTCAACAGTGGCATTTTCCACCAAACCC[A/T]AACATCCGTCGGCGATGCCCACTACTGAGAAGACAAAAAAAAGAAAAAGG
Long Flanking Sequence:
TTCCGTTGGTAATCCTGCAATTTAGGACGCAGCTTCTGGTTTGTCGACAGATACTTTATATGTTACTTGTCGCCACCTACTGGCATACAGGTGTAATTGTTACTTTCAAAACATTATTAACTCTATTTTAAAGTTTTTATCCAAACAATAAACTATAATCTCAGTACTTTTTTGATCATTTGAATGTTTGTATCACAAAAATAAATCAAGTAAACATAATAAACAAATAAAATATACAAAACTACTACTTTGTATTTGTCAAAGGCTTAATAAGTATATGTTAATCACTGTCTTTGTTTTCAGTGTTTTTGTTTAAAAATAATGAGGTCGCAGTCTTTTAATTTAATTGACTTTAAACAAGTCGTGCAGCTCTGAAATGTACATTCATGCATTTCACAGGAAAACCAGTGAATAGTTTAGTGTGTTGGACAATTGTACTATATTAGATCATCATGCACTGACATCACTCTTGCTCAACAGTGGCATTTTCCACCAAACCC[A/T]AACATCCGTCGGCGATGCCCACTACTGAGAAGACAAAAAAAAGAAAAAGGAAGGGCAAAGGAAAAGGCAGGGGGAATAAGAAGAACCTCTGCGAGGAGGAATACAAAGATTTCTGCATTCATGGAGTGTGTCATTATCTGCGGGATTTACGCACTCATTCTTGTGTGTAAGTTTCATGCAGTTCTATTGTCTTAGTAATCCAAAAATGACAATTCAGTCATTGTTTACTTCCCTCAAGTTGTTCCAAACCTGTCTGAGTTTCTTTCTTCCGTTAAACACAAAAGGAGATATTTTTAAGAATGTTGGAAACTAGTAACCATTAACTTCCATTGTTTTTTTCTATACTATAATTGTCAATAGTTTCCAACATTCTTCAAAATGTTTTCCTTTTATGTTTAATAGAATAATAAAAAACATAACGTTTTGGAACCAAGCATGAGTAAGGGTGAGGTAAAGGATGGTAAAACTTTCATTTTATTAATTTAGTAGATACTTTTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11891
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010193 | Nonsense | 138 | 239 | 3 | 6 |
ENSDART00000130676 | Nonsense | 4 | 113 | 1 | 4 |
ENSDART00000130820 | Nonsense | 162 | 263 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 21 (position 28910149)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 30129393 |
GRCz11 | 21 | 30166088 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAAAAAGGAAGGRCAAAGGAAAAGGCAGGGGGAATAAGAAGAACCTCTG[C/A]RAGGAGGAATACAAAGATTTCTGCATTCATGGAGTGTGTCAKTATCWGCG
Long Flanking Sequence:
GTAATTGTTACTTTCAAAACATTATTAACTCTATTTTAAAGTTTTTATCCAAACAATAAACTATAATCTCAGTACTTTTTTGATCATTTGAATGTTTGTATCACAAAAATAAATCAAGTAAACATAATAAACAAATAAAATATACAAAACTACTACTTTGTATTTGTCAAAGGCTTAATAAGTATATGTTAATCACTGTCTTTGTTTTCAGTGTTTTTGTTTAAAAATAATGAGGTCGCAGTCTTTTAATTTAATTGACTTTAAACAAGTCGTGCAGCTCTGAAATGTACATTCATGCATTTCACAGGAAAACCAGTGAATAGTTTAGTGTGTTGGACAATTGTACTATATTAGATCATCATGCACTGACATCACTCTTGCTCAACAGTGGCATTTTCCACCAAACCCAAACATCCGTCGGCGATGCCCACTACTGAGAAGACAAAAAAAAGAAAAAGGAAGGGCAAAGGAAAAGGCAGGGGGAATAAGAAGAACCTCTG[C/A]GAGGAGGAATACAAAGATTTCTGCATTCATGGAGTGTGTCATTATCTGCGGGATTTACGCACTCATTCTTGTGTGTAAGTTTCATGCAGTTCTATTGTCTTAGTAATCCAAAAATGACAATTCAGTCATTGTTTACTTCCCTCAAGTTGTTCCAAACCTGTCTGAGTTTCTTTCTTCCGTTAAACACAAAAGGAGATATTTTTAAGAATGTTGGAAACTAGTAACCATTAACTTCCATTGTTTTTTTCTATACTATAATTGTCAATAGTTTCCAACATTCTTCAAAATGTTTTCCTTTTATGTTTAATAGAATAATAAAAAACATAACGTTTTGGAACCAAGCATGAGTAAGGGTGAGGTAAAGGATGGTAAAACTTTCATTTTATTAATTTAGTAGATACTTTTGTCCATAATAATTTGCTGATATCTTTCACCTGTTTAAAACCAGTTTGAGTTTCTGTCTTCTGTTGAACAAAAAAGCAAGATATTCTGAAGAATGT
Associated Phenotype:
Not determined